Vent arrangement for respiratory device

Abstract

A vent arrangement for a respiratory pressure therapy device may include one or a plurality of vents configured with a variable aperture for communicating a flow of breathable gas. The vent arrangement may be configured with a cross section profile exposed to the flow of breathable gas communicating through the vent that does not change as the aperture size changes. A vent arrangement may include a plurality of the vents and the aperture size of each vent may be controlled independently or together, and may be controlled according to one or more input signals from one or more sensors. Examples of suitable input signals include flow, pressure, noise, accelerometer outputs, orientation of a patient or presence of any obstructions. A patient interface or an air circuit may include the vent arrangement, or the vent arrangement may be configured to connect with a patient interface or an air circuit.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]The present application is a national phase entry under 35 U.S.C. § 371 of International Application No. PCT / AU2014 / 000263 filed Mar. 14, 2014, published in English, which claims priority from Australian Provisional Patent Application No. 2013900885, filed Mar. 14, 2013 and Australian Provisional Patent Application No. 2013903088, filed Aug. 16, 2013, all of which are hereby incorporated herein by reference.BACKGROUND OF THE INVENTION[0002](1) Field of the Invention[0003]The present technology relates to one or more of the detection, diagnosis, treatment, prevention and amelioration of respiratory-related disorders. In particular, the present technology relates to medical devices or apparatus, and their use.[0004](2) Description of the Related Art[0005]3.2.1 Human Respiratory System and its Disorders[0006]The respiratory system of the body facilitates gas exchange. The nose and mouth form the entrance to the airways of a patient.[0007]The...

AI Technical Summary

Benefits of technology

[0048]The ResMed Elisée™ 150 ventilator and ResMed VS III™ ventilator may provide support for invasive and non-invasive dependent ventilation suitable for adult or paediatric patients for treating a number of conditions. These ventilators provide volumetric and barometric ventilation modes with a single or double limb circuit.

[0054]The use of a humidifier with a flow generator or RPT device and the patient interface produces humidified gas that minimizes drying of the nasal mucosa and increases patient airway comfort. In addition, in cooler climates warm air applied generally to the face area in and about the patient interface is more comfortable than cold air.

[0059]The present technology relates to devices that may be used medically such as for the diagnosis, amelioration, treatment, and / or prevention of respiratory disorders, and may have one or more features for improved comfort, cost, efficacy, ease of use and / or manufacturability.

[0078]Some versions of the present technology may include a control method, such as a control method of an apparatus for adjusting a flow of exhaust gas from a patient interface. The control method may include generating with a sensor a signal indicative of disruption attributable to a flow of exhaust gas through one or more vents from a patient interface. The one or more vents may be adapted for a plurality of different venting configurations. The control method may further include adjusting with a controller the one or more vents to one of the plurality of different venting configurations based on the signal, whereby disruption to a user and / or bed-partner of the user may be reduced.

Problems solved by technology

For other forms of therapy, such as the delivery of oxygen, the patient interface may not include a seal sufficient to facilitate delivery to the airways of a supply of gas at a positive pressure of about 10 cm H2O.

The design of a patient interface presents a number of challenges.

As a consequence of these challenges, some masks suffer from beimg one or more of obtrusive, aesthetically undesirable, costly, poorly fitting, difficult to use and uncomfortable especially when worn for long periods of time or when a patient is unfamiliar with a system.

For example, masks designed solely for aviators, mask designed as part of personal protection equipment (e.g. filter masks), SCUBA masks or for the administration of anaesthetics may be tolerable for their original application, but nevertheless be undesirably uncomfortable to be worn for extended periods of time, e.g. several hours.

If a mask is uncomfortable, or difficult to use a patient may not comply with therapy.

Since it is often recommended that a patient regularly wash their mask, if a mask is difficult to clean (e.g. difficult to assemble or disassemble), patients may not clean their mask and this may impact on patient compliance.

For example, a seal on swimming goggles that overlays a patient's forehead may not be appropriate to use on a patient's nose.

Like the previous style of seal forming portion, if the match between the face and the mask is not good, additional force may be required to effect a seal, or the mask may leak.

Furthermore, if the shape of the seal-forming portion does not match that of the patient, it may crease or buckle in use, giving rise to leaks.

Some patients may find it inconvenient to constantly apply and remove an adhesive to their face.

Many such harnesses suffer from being one or more of ill-fitting, bulky, uncomfortable and awkward to use.

Many such vents are noisy.

Others may block in use and provide insufficient washout.

Delivery of a flow of breathable gas without humidification may cause drying of airways.

Room-based systems (e.g. a sauna, an air conditioner, an evaporative cooler), for example, may also humidify air that is breathed in by the patient, however they would also humidify and / or heat the entire room, which may cause discomfort to the occupants.

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